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Learning Oriented Physiotherapy - a New Approach

The Effect of Learning Oriented Physiotherapy on Health-Related Functioning and Quality of Life in Patients With Various Anxiety Disorders

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02194036
Acronym
LOF
Enrollment
81
Registered
2014-07-18
Start date
2014-08-31
Completion date
2017-09-01
Last updated
2018-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Agitation, Anxiety, Depression, Dizziness, Fatigue, Numbness, Pain, Sleep Disturbances

Keywords

Ownership of body, Bodily and mental balance, Learning, Body image, Sensations, Expectations

Brief summary

Outpatients that suffer from different anxiety disorders may have physical ailments that negatively affect daily life functioning and quality of life. LOF is a physical therapy approach focusing on the link between bodily and mental balance and through defined, but simple movements, patients are expected to learn how to cope and reduce health complaints. This study aims to investigate the short- and longterm effect of LOF compared to other standardized psychiatric treatments given in the clinic on levels of anxiety and depression, health related function and quality of life.

Interventions

BEHAVIORALLearning Oriented Physiotherapy

Clinical practice based on a new understanding of the neurobiological basis for the interaction between body and mind, the foundation of learning and what is needed to bring about change of behavior.

BEHAVIORALWidely Recognized Psychiatric Treatment

Standard recognized psychiatric treatment tailored to individual needs.

Sponsors

Health North Trøndelag
CollaboratorUNKNOWN
Health Møre and Romsdal
CollaboratorUNKNOWN
South Coast Hospital Hf Dps Aust-Agder Units Arendal
CollaboratorUNKNOWN
Helse Nord-Trøndelag HF
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

The study population will be recruited among patients referred to three Norwegian psychiatric outpatient clinics for anxiety-like conditions. The same criteria for inclusion and exclusion will be applied for the experimental and active comparator group. Inclusion Criteria: Participants should be * 18 years or older * able to read, write and speak Norwegian * understand the project information and consent

Exclusion criteria

Participants should not * have ongoing substance abuse or addiction. * be psychotic.

Design outcomes

Primary

MeasureTime frameDescription
Changes in Health Related Quality of Life (HRoQL)From baseline to 6, 12 and 18 months of follow-upIn this study HRoQL will be measured by the validated EQ5D questionnaire

Secondary

MeasureTime frameDescription
Changes in Levels of Anxiety and DepressionFrom baseline to 6, 12 and 18 months of follow-upHospital Anxiety and Depression Scale (HAD) will be used as instrument to assess levels and changes in anxiety and depression over time .

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026